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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

3-Butyn-1-amine, 4-(trimethylsilyl)-

NCCC#C[Si](C)(C)C Request for Quotation
Chemical Name: 3-Butyn-1-amine, 4-(trimethylsilyl)-
CAS Number: 183208-71-1
Product Number: AG00I1EQ(AGN-PC-02IPVA)
Synonyms:
MDL No:
Molecular Formula: C7H15NSi
Molecular Weight: 141.2862

Identification/Properties

Computed Properties
Molecular Weight:
141.289g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
141.097g/mol
Monoisotopic Mass:
141.097g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
132
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Trimethylsilyl)-3-butyn-1-amine is a versatile compound widely employed in chemical synthesis due to its unique chemical properties. This compound serves as a valuable building block for the preparation of various functionalized organic molecules and heterocycles. In organic synthesis, the presence of the trimethylsilyl group enhances the reactivity and selectivity of the amine group, making it a powerful tool for the introduction of nitrogen-containing functionalities into complex molecular structures. Additionally, the alkyne functionality in 4-(Trimethylsilyl)-3-butyn-1-amine enables it to participate in diverse synthetic transformations, including Sonogashira couplings, cycloadditions, and cross-coupling reactions, leading to the formation of highly functionalized molecules with potential applications in pharmaceuticals, materials science, and agrochemicals. Its strategic incorporation in synthetic pathways enables chemists to access a wide array of structurally diverse compounds, thus facilitating the development of novel chemical entities with unique properties and functions.